HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171651975_171651976del , CM000663.2:g.171651975_171651976del | GRCh38 |
NC_000001.10:g.171621115_171621116del , CM000663.1:g.171621115_171621116del | GRCh37 |
NC_000001.9:g.169887738_169887739del | NCBI36 |
NG_008859.1:g.5658_5659del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.604+32_604+33del MANE Select | ENSP00000037502.5:n.604+32_604+33del | |
ENST00000638471.1:c.130+506_130+507del | ENSP00000491206.1:n.130+506_130+507del | |
ENST00000037502.10:c.604+32_604+33del | ENSP00000037502.5:n.604+32_604+33del | |
ENST00000614688.1:c.604+32_604+33del | ENSP00000478680.1:n.604+32_604+33del | |
NM_000261.1:c.604+32_604+33del | NP_000252.1:n.604+32_604+33del | |
NM_000261.2:c.604+32_604+33del MANE Select | NP_000252.1:n.604+32_604+33del |